Literature DB >> 22139735

The prognostic difference of monoallelic versus biallelic deletion of 13q in chronic lymphocytic leukemia.

Ravin Garg1, William Wierda, Alessandra Ferrajoli, Lynne Abruzzo, Sherry Pierce, Susan Lerner, Michael Keating, Susan O'Brien.   

Abstract

BACKGROUND: Fluorescence in situ hybridization can detect genomic abnormalities in up to 80% of cases and provides prognostic information on patients with chronic lymphocytic leukemia (CLL). Although 13q deletion as the sole abnormality has been found to confer a favorable prognosis, there are little data as to whether there is a difference in prognostic value between monoallelic versus biallelic deletion of 13q.
METHODS: The authors reviewed the electronic database for patients with CLL who carried the 13q deletion as the sole abnormality and presented to The University of Texas MD Anderson Cancer Center (MDACC). Untreated patients were separated into 2 groups: those having monoallelic versus those with biallelic deletion of 13q. Using Mann-Whitney, chi-square, and Kaplan-Meier analysis, the baseline quantitative and qualitative variables for each group, along with the time from presentation to MDACC to treatment, were compared.
RESULTS: A total of 176 patients were identified; 143 patients had a monoallelic deletion of 13q, whereas 33 patients had a biallelic deletion. The only significantly different values between the groups were albumin (4.5 g/dL vs 4.4 g/dL; P = .01) and zeta-chain-associated protein kinase 70 (ZAP70) expression (1.7% vs 4.8%; P = .010). The median time from fluorescence in situ hybridization analysis to treatment in both the monoallelic and biallelic groups had not been reached (P = not significant).
CONCLUSIONS: Except for inconsequential differences in albumin and ZAP70 expression, there was no difference in the baseline characteristics between patients with CLL who had monoallelic or biallelic deletion of 13q. In addition, there was no significant difference in endpoints, including time to treatment.
Copyright © 2011 American Cancer Society.

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Year:  2011        PMID: 22139735      PMCID: PMC4535912          DOI: 10.1002/cncr.26593

Source DB:  PubMed          Journal:  Cancer        ISSN: 0008-543X            Impact factor:   6.860


  25 in total

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Authors:  K R Rai; A Sawitsky; E P Cronkite; A D Chanana; R N Levy; B S Pasternack
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2.  V(H) mutation status, CD38 expression level, genomic aberrations, and survival in chronic lymphocytic leukemia.

Authors:  Alexander Kröber; Till Seiler; Axel Benner; Lars Bullinger; Elsbeth Brückle; Peter Lichter; Hartmut Döhner; Stephan Stilgenbauer
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3.  Chronic lymphocytic leukaemia profiled for prognosis using a fluorescence in situ hybridisation panel.

Authors:  K S Reddy
Journal:  Br J Haematol       Date:  2006-03       Impact factor: 6.998

4.  Genome-wide analysis of DNA copy number changes and LOH in CLL using high-density SNP arrays.

Authors:  Dietmar Pfeifer; Milena Pantic; Ilona Skatulla; Justyna Rawluk; Clemens Kreutz; Uwe M Martens; Paul Fisch; Jens Timmer; Hendrik Veelken
Journal:  Blood       Date:  2006-10-19       Impact factor: 22.113

5.  Frequent deletions and down-regulation of micro- RNA genes miR15 and miR16 at 13q14 in chronic lymphocytic leukemia.

Authors:  George Adrian Calin; Calin Dan Dumitru; Masayoshi Shimizu; Roberta Bichi; Simona Zupo; Evan Noch; Hansjuerg Aldler; Sashi Rattan; Michael Keating; Kanti Rai; Laura Rassenti; Thomas Kipps; Massimo Negrini; Florencia Bullrich; Carlo M Croce
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6.  Genomic aberrations and survival in chronic lymphocytic leukemia.

Authors:  H Döhner; S Stilgenbauer; A Benner; E Leupolt; A Kröber; L Bullinger; K Döhner; M Bentz; P Lichter
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Review 7.  Chromosome aberrations in B-cell chronic lymphocytic leukemia: reassessment based on molecular cytogenetic analysis.

Authors:  H Döhner; S Stilgenbauer; K Döhner; M Bentz; P Lichter
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8.  ZAP-70 expression as a surrogate for immunoglobulin-variable-region mutations in chronic lymphocytic leukemia.

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9.  Retinoblastoma gene deletions in B-cell chronic lymphocytic leukemia.

Authors:  Y Liu; D Grandér; S Söderhäll; G Juliusson; G Gahrton; S Einhorn
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10.  Chromosome anomalies detected by interphase fluorescence in situ hybridization: correlation with significant biological features of B-cell chronic lymphocytic leukaemia.

Authors:  Gordon W Dewald; Stephanie R Brockman; Sarah F Paternoster; Nancy D Bone; Judith R O'Fallon; Cristine Allmer; Charles D James; Diane F Jelinek; Renee C Tschumper; Curtis A Hanson; Rajiv K Pruthi; Thomas E Witzig; Timothy G Call; Neil E Kay
Journal:  Br J Haematol       Date:  2003-04       Impact factor: 6.998

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Review 2.  Prognostic Factors in the Era of Targeted Therapies in CLL.

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3.  Which prognostic marker is responsible for the clinical heterogeneity in CLL with 13q deletion?

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Journal:  Mol Cytogenet       Date:  2021-01-06       Impact factor: 2.009

Review 4.  Genetic abnormalities in chronic lymphocytic leukemia: where we are and where we go.

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Journal:  Biomed Res Int       Date:  2014-05-22       Impact factor: 3.411

5.  Characteristics of chronic lymphocytic leukemia in Senegal.

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6.  Monoallelic and biallelic deletions of 13q14 in a group of CLL/SLL patients investigated by CGH Haematological Cancer and SNP array (8x60K).

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7.  Chromosomal aberrations detected by Fluorescence in situ hybridization in 344 Brazilian chronic lymphocytic leukemia patients.

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Review 8.  Tumor Suppressors in Chronic Lymphocytic Leukemia: From Lost Partners to Active Targets.

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